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Biogenic impact on materials
(2011)
Materials as constituents of products or components of technical systems rarely exist in isolation and many must cope with exposure in the natural world. This chapter describes methods that simulate how a material is influenced through contact with living systems such as microorganisms and arthropods. Both unwanted and desirable interactions are considered. This biogenic impact on materials is intimately associated with the environment to which the material is exposed (Materials-Environment Interaction, Chap. 15). Factors such as moisture, temperature and availability of food sources all have a significant influence on biological systems. Corrosion (Chap. 12) and wear (Chap. 13) can also be induced or enhanced in the presence of microorganisms. Section 14.1 introduces the categories between desired (biodegradation) and undesired (biodeterioration) biological effects on materials. It also introduces the role of biocides for the protection of materials. Section 14.2 describes the testing of wood as a building material especially against microorganisms and insects. Section 14.3 characterizes the test methodologies for two other groups of organic materials, namely polymers (Sect. 14.3.1) and paper and textiles (Sect. 14.3.2). Section 14.4 deals with the susceptibility of inorganic materials such as metals (Sect. 14.4.1), concrete (Sect. 14.4.2) and ceramics (Sect. 14.4.3) to biogenic impact. Section 14.5 treats the testing methodology concerned with the performance of coatings and coating materials. In many of these tests specific strains of organisms are employed. It is vital that these strains retain their ability to utilize/attack the substrate from which they were isolated, even when kept for many years in the laboratory. Section 14.6 therefore considers the importance of maintaining robust and representative test organisms that are as capable of utilizing a substrate as their counterparts in nature such that realistic predictions of performance can be made.
Alarm response triggered by physical stimuli is wide spread in termites but executed in several different behavioural patterns. The drywood and subterranean termite species tested in this study differed significantly by either head-drumming or jerking when stimulated by light, air-flow, or air borne Sound stimuli. Nevertheless, differences may have a common evolutionary base. Repetitive stimuli of the same quality led to reduced responses over time, which was interpreted as habituation behaviour, a simple form of learning. Adaptation as alternative explanation was ruled out because when termites were subjected with a dis-habituation-stimulus followed by the original stimulus full Response occurred again to this stimulus.
Subterranean termites moving in the peripheral tubular network of their foraging area need to distinguish the trail direction. In a natural gallery or tunnel network of Reticulitermes flavipes the branches at bifurcations generally have an acute angle between them. the resulting obtuse angle from the main trail leading into a branch is preferred by commuting termites. In experiments with artificial gallery forks, termites returning from a food source only neglected the trail junction leading to the nest and preferred the trail to a second food source if the angle to the nest was acute. A right angle to the nest was preferred over a straight way leading to a second food source. This preference to the nest increased when the three branches at trifurcations were arranged equi-angular. This preferred orientation could be attributed to attracting odours from close-by gallery material. Additionally, R. flavipes moved more slowly towards a food source consisting of pine wood than on the way back to the nest, as was shown in artificial one-way galleries. However, the significance of this speed difference remains uncertain because the speed of a homing termite in an artificially reversed trail does not slow down to the speed of a food foraging termite.
The surface of many termite gut flagellates is colonized with a dense layer of bacteria, yet little is known about the evolutionary relationships of such ectosymbionts and their hosts. Here we investigated the molecular phylogenies of devescovinid flagellates (Devescovina spp.) and their symbionts from a wide range of dry-wood termites (Kalotermitidae). From species-pure flagellate suspensions isolated with micropipettes, we obtained SSU rRNA gene sequences of symbionts and host. Phylogenetic analysis showed that the Devescovina spp. present in many species of Kalotermitidae form a monophyletic group, which includes also the unique devescovinid flagellate Caduceia versatilis. All members of this group were consistently associated with a distinct lineage of Bacteroidales, whose location on the cell surface was confirmed by fluorescence in situ hybridization. The well-supported congruence of the phylogenies of devescovinids and their ectosymbionts documents a strict cospeciation. In contrast, the endosymbionts of the same flagellates (´Endomicrobia´) were clearly polyphyletic and must have been acquired independently by horizontal transfer from other flagellate lineages. Also the Bacteroidales ectosymbionts of Oxymonas flagellates present in several Kalotermitidae belonged to several distantly related lines of descent, underscoring the general perception that the evolutionary history of flagellate-bacteria symbioses in the termite gut is complex.